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   <dc:title>Analysis of histology-agnostic targets among soft tissue and bone sarcomas in the AACR GENIE database</dc:title>
   <dc:creator>Carmagnani Pestana, Roberto</dc:creator>
   <dc:creator>Serrano Garcia, César</dc:creator>
   <dc:contributor>Institut Català de la Salut</dc:contributor>
   <dc:contributor>[Pestana RC] Hospital Israelita Albert Einstein, São Paulo, Brazil. [Serrano C] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Sarcoma Translational Research Program, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain</dc:contributor>
   <dc:contributor>Vall d'Hebron Barcelona Hospital Campus</dc:contributor>
   <dc:subject>Tumors de parts toves - Tractament</dc:subject>
   <dc:subject>Marcadors tumorals</dc:subject>
   <dc:subject>DISEASES::Neoplasms::Neoplasms by Site::Soft Tissue Neoplasms</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Biological Factors::Biomarkers::Biomarkers, Tumor</dc:subject>
   <dc:subject>ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de los tejidos blandos</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::factores biológicos::biomarcadores::marcadores tumorales</dc:subject>
   <dc:description>Precision medicine; Sarcoma; Tissue-agnostic biomarker</dc:description>
   <dc:description>Medicina de precisió; Sarcoma; Biomarcador agnòstic dels teixits</dc:description>
   <dc:description>Medicina de precisión; Sarcoma; Biomarcador agnóstico de tejido</dc:description>
   <dc:description>Background: The development of novel therapies for patients with sarcoma is challenging due to the rarity and diversity of these mesenchymal neoplasms. Hence, histology-agnostic approvals can be of particular interest for the treatment of patients with soft tissue and bone sarcoma.&#xd;
&#xd;
Methods: We queried the American Association for Cancer Research (AACR) Project Genomics Evidence Neoplasia Information Exchange (GENIE) database Cohort v12.0-Public to investigate the prevalence of currently Food and Drug Administration (FDA)-approved and other potentially actionable histology-agnostic alterations in patients with soft tissue and bone sarcoma. Targets were identified by a literature review by the authors. Results are presented for each cohort identified in the GENIE database, namely: (1) soft tissue sarcoma (STS), (2) gastrointestinal stromal tumor (GIST), (3) bone sarcoma, (4) uterine sarcoma, and (5) breast sarcoma.&#xd;
&#xd;
Results: We identified 7,512 samples of 6,955 patients with sarcoma in the AAACR GENIE database v12.0-Public. Molecular alterations that could lead to the clinical use of a currently approved histology-agnostic therapy were identified in 2.1% of sarcomas (2.6% STS, 1.3% GIST, 1.4% bone, 2.7% uterine, and 0% breast). In addition, 2.9% of patients could be eligible for future histology-agnostic approvals. These specific mutations, fusions, and amplifications occurred in multiple histotypes in all cohorts.&#xd;
&#xd;
Discussion: Exploring a public large-scale genomic database, we identified that 5% of patients with sarcoma could be eligible for current histology-agnostic FDA-approved drugs or future potential histology-agnostic indications. These actionable alterations were present in a wide variety of histologies in soft tissue and bone sarcomas, highlighting that next-generation sequencing can be considered for patients with advanced sarcoma to guide treatment strategies.</dc:description>
   <dc:date>2023-03-08T13:24:45Z</dc:date>
   <dc:date>2023-03-08T13:24:45Z</dc:date>
   <dc:date>2023-01-18</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>Pestana RC, Serrano C. Analysis of histology-agnostic targets among soft tissue and bone sarcomas in the AACR GENIE database. Front Oncol. 2023 Jan 18;12:1079909.</dc:identifier>
   <dc:identifier>2234-943X</dc:identifier>
   <dc:identifier>https://hdl.handle.net/11351/9128</dc:identifier>
   <dc:identifier>10.3389/fonc.2022.1079909</dc:identifier>
   <dc:identifier>36741731</dc:identifier>
   <dc:identifier>000922398300001</dc:identifier>
   <dc:identifier>http://hdl.handle.net/11351/9128</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Frontiers in Oncology;12</dc:relation>
   <dc:relation>https://doi.org/10.3389/fonc.2022.1079909</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Frontiers Media</dc:publisher>
   <dc:source>Scientia</dc:source>
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